Answer:
Option (C)
Explanation:
Blood smears usually refers to the blood test that is being conducted in order to determine if there is any abnormality or irregularity in the blood cells. This test is conducted in the laboratories by using the slides.
After the test is done, these slides of blood smears are usually disposed of according to the instruction given by the teachers. It is because these slides have sharp edges and must be carefully handled. It can cause cut in the fingers and as these slides are comprised of infectious substances, it can affect other individuals, causing various types of diseases.
Thus, they must not be disposed of here and there, rather they should be disposed of according to the teacher's instruction.
Hence, the correct answer is option (C).
Explanation:
A single nucleotide-pair substitution missense mutation causes a change of a single amino acid into another. Aa a result, the produced protein will have an almost normal sequence except for one amino acid.
On the other hand, a frameshift mutation changes the Open Reading Frame (ORF) of the ribosome. The ribosome moves along the mRNA every three nucleotides (codons) and translates them into amino acids that will form the nascent protein. If there is a frameshift mutation (an insertion or deletion of a number of nucleotides not multiple of three) the ribosome will "read" the mRNA differently and will identify different codons than the wild-type sequence, so a large number of amino acids will be different in the mutated protein.
The variety of all life forms on Earth.
Differences of chilopoda and diplopoda are above .
A trisomy is a chromosomal condition characterized by an additional chromosome. A person with a trisomy has 47 chromosomes instead of 46.
Trisomy means the presence of an extra chromosome in some or all of the body's cells. This results in a total of three copies of that chromosome instead of the normal two copies. For example, Down syndrome (trisomy 21) is caused by having three copies of chromosome 21 instead of the usual two copies.
This genetic condition is the result of a genetic mutation where your cells don't divide as they should. You can't prevent this abnormality from happening during cell division.
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